NDC 27808-091 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 2.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC27808-091

Product details

Brand name
Dexmethylphenidate Hydrochloride
Generic name
Dexmethylphenidate hydrochloride
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207901
Marketed since
November 30, 2001
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
27808-091-01100 TABLET in 1 BOTTLE, PLASTIC (27808-091-01)Nov 30, 2001

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